Title 21

PART 630

Part 630 - Requirements For Blood And Blood Components Intended For Transfusion Or For Further Manufacturing Use

PART 630 - REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE Authority:21 U.S.C. 321, 331, 351, 352, 355, 360, 371; 42 U.S.C. 216, 262, 264. Source:66 FR 31176, June 11, 2001, unless otherwise noted.

21:7.0.1.1.6.1SUBPART A
Subpart A - General Provisions
21:7.0.1.1.6.1.1.1SECTION 630.1
   630.1 Purpose and scope.
21:7.0.1.1.6.1.1.2SECTION 630.3
   630.3 Definitions.
21:7.0.1.1.6.2SUBPART B
Subpart B - Donor Eligibility Requirements
21:7.0.1.1.6.2.1.1SECTION 630.5
   630.5 Medical supervision.
21:7.0.1.1.6.2.1.2SECTION 630.10
   630.10 General donor eligibility requirements.
21:7.0.1.1.6.2.1.3SECTION 630.15
   630.15 Donor eligibility requirements specific to Whole Blood, Red Blood Cells and Plasma collected by apheresis.
21:7.0.1.1.6.2.1.4SECTION 630.20
   630.20 Exceptions for certain ineligible donors.
21:7.0.1.1.6.2.1.5SECTION 630.25
   630.25 Exceptions from certain donor eligibility requirements for infrequent plasma donors.
21:7.0.1.1.6.2.1.6SECTION 630.30
   630.30 Donation suitability requirements.
21:7.0.1.1.6.2.1.7SECTION 630.35
   630.35 Requalification of previously deferred donors.
21:7.0.1.1.6.3SUBPART C
Subpart C - Donor Notification
21:7.0.1.1.6.3.1.1SECTION 630.40
   630.40 Requirements for notifying deferred donors.